Cryo-Electron Tomography Elucidates the Molecular Architecture of Treponema pallidum , the Syphilis Spirochete

Author:

Izard Jacques12,Renken Christian3,Hsieh Chyong-Ere3,Desrosiers Daniel C.4,Dunham-Ems Star4,La Vake Carson4,Gebhardt Linda L.3,Limberger Ronald J.3,Cox David L.5,Marko Michael3,Radolf Justin D.46

Affiliation:

1. Department of Molecular Genetics, The Forsyth Institute, Boston, Massachusetts 02135

2. Harvard School of Dental Medicine, Boston, Massachusetts 02115

3. Wadsworth Center, New York State Department of Health, Albany, New York 12201

4. Departments of Medicine

5. Division of STD Prevention, Laboratory Reference and Research Branch, Centers for Disease Control and Prevention, Atlanta, Georgia 30333

6. Genetics and Developmental Biology, University of Connecticut Health Center, Farmington, Connecticut 06030

Abstract

ABSTRACT Cryo-electron tomography (CET) was used to examine the native cellular organization of Treponema pallidum , the syphilis spirochete. T. pallidum cells appeared to form flat waves, did not contain an outer coat and, except for bulges over the basal bodies and widening in the vicinity of flagellar filaments, displayed a uniform periplasmic space. Although the outer membrane (OM) generally was smooth in contour, OM extrusions and blebs frequently were observed, highlighting the structure's fluidity and lack of attachment to underlying periplasmic constituents. Cytoplasmic filaments converged from their attachment points opposite the basal bodies to form arrays that ran roughly parallel to the flagellar filaments along the inner surface of the cytoplasmic membrane (CM). Motile treponemes stably attached to rabbit epithelial cells predominantly via their tips. CET revealed that T. pallidum cell ends have a complex morphology and assume at least four distinct morphotypes. Images of dividing treponemes and organisms shedding cell envelope-derived blebs provided evidence for the spirochete's complex membrane biology. In the regions without flagellar filaments, peptidoglycan (PG) was visualized as a thin layer that divided the periplasmic space into zones of higher and lower electron densities adjacent to the CM and OM, respectively. Flagellar filaments were observed overlying the PG layer, while image modeling placed the PG-basal body contact site in the vicinity of the stator-P-collar junction. Bioinformatics and homology modeling indicated that the MotB proteins of T. pallidum , Treponema denticola , and Borrelia burgdorferi have membrane topologies and PG binding sites highly similar to those of their well-characterized Escherichia coli and Helicobacter pylori orthologs. Collectively, our results help to clarify fundamental differences in cell envelope ultrastructure between spirochetes and gram-negative bacteria. They also confirm that PG stabilizes the flagellar motor and enable us to propose that in most spirochetes motility results from rotation of the flagellar filaments against the PG.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

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